Jean-Baka Domelevo Entfellner
Overview
Explore the profile of Jean-Baka Domelevo Entfellner including associated specialties, affiliations and a list of published articles.
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25
Citations
209
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Recent Articles
21.
Ghouila A, Siwo G, Domelevo Entfellner J, Panji S, Button-Simons K, Davis S, et al.
Genome Res
. 2018 Apr;
28(5):759-765.
PMID: 29650552
Scientific research plays a key role in the advancement of human knowledge and pursuit of solutions to important societal challenges. Typically, research occurs within specific institutions where data are generated...
22.
Gurwitz K, Aron S, Panji S, Maslamoney S, Fernandes P, Judge D, et al.
PLoS Comput Biol
. 2017 Oct;
13(10):e1005715.
PMID: 28981516
Africa is not unique in its need for basic bioinformatics training for individuals from a diverse range of academic backgrounds. However, particular logistical challenges in Africa, most notably access to...
23.
Wanet A, Caruso M, Domelevo Entfellner J, Najar M, Fattaccioli A, Demazy C, et al.
Stem Cells
. 2017 Aug;
35(10):2184-2197.
PMID: 28795454
Increasing evidence supports that modifications in the mitochondrial content, oxidative phosphorylation (OXPHOS) activity, and cell metabolism influence the fate of stem cells. However, the regulators involved in the crosstalk between...
24.
Kroger W, Mapiye D, Domelevo Entfellner J, Tiffin N
BMC Med Genomics
. 2016 Nov;
9(1):66.
PMID: 27846842
Background: Systemic Lupus Erythematosus (SLE) is a complex, multi-systemic, autoimmune disease for which the underlying aetiological mechanisms are poorly understood. The genetic and molecular processes underlying lupus have been extensively...
25.
Bendou H, Domelevo Entfellner J, van Heusden P, Gamieldien J, Tiffin N
BMC Res Notes
. 2016 Mar;
9:144.
PMID: 26945860
Background: The National Institutes of Health (USA) has committed 5 years of funding to the Bioinformatics Network of the Human Heredity and Health in Africa initiative. This pan-African network aims...
26.
Bosch J, Noubiap J, Dandara C, Makubalo N, Wright G, Domelevo Entfellner J, et al.
OMICS
. 2014 Aug;
18(11):705-10.
PMID: 25162826
Mutations in the GJB2 gene, encoding connexin 26, could account for 50% of congenital, nonsyndromic, recessive deafness cases in some Caucasian/Asian populations. There is a scarcity of published data in...